Associated Papers
The unveiled face of IEI: Children Cancer Hospital-Egypt (CCHE-57357) experience.
Radwan N et al.
Frontiers in Immunology, 2025
Genetic screening of male patients with primary hypogammaglobulinemia can guide diagnosis and clinical management.
Vince N et al.
Human Immunology, 2018
Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene.
Tóth B et al.
Journal of Clinical Immunology, 2015
The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation.
Overwater E et al.
European Journal of Pediatrics, 2014
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